Is Hypertrophic Cardiomyopathy Always a Familial and Inherited Disease?
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu dopisy, práce podpořená grantem
PubMed
37301765
PubMed Central
PMC10356023
DOI
10.1161/jaha.122.028974
Knihovny.cz E-zdroje
- Klíčová slova
- familial, genetics, hypertrophic cardiomyopathy, inheritance,
- MeSH
- familiární hypertrofická kardiomyopatie * diagnóza genetika terapie MeSH
- hypertrofická kardiomyopatie * diagnóza genetika MeSH
- lidé MeSH
- mutace MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- dopisy MeSH
- práce podpořená grantem MeSH
Zobrazit více v PubMed
Maron BJ. Clinical course and management of hypertrophic cardiomyopathy. N Engl J Med. 2018;379:655–666. doi: 10.1056/NEJMra1710575 PubMed DOI
Chou C, Chin MT. Pathogenic mechanisms of hypertrophic cardiomyopathy beyond sarcomere dysfunction. Int J Mol Sci. 2021;22:8933. doi: 10.3390/ijms22168933 PubMed DOI PMC
Braunwald E, Lambrew CT, Rockoff SD, Ross J Jr, Morrow AG. Idiopathic hypertrophic subaortic stenosis. I. A description of the disease based upon an analysis of 64 patients. Circulation. 1964;30:3–119. doi: 10.1161/01.cir.29.5s4.iv-3 PubMed DOI
Ingles J, Burns C, Bagnall RD, Lam L, Yeates L, Sarina T, Puranik R, Briffa T, Atherton JJ, Driscoll T, et al. Nonfamilial hypertrophic cardiomyopathy: prevalence, natural history, and clinical implications. Circ Cardiovasc Genet. 2017;10:e001620. doi: 10.1161/CIRCGENETICS.116.001620 PubMed DOI
Maron BA, Wang RS, Carnethon MR, Rowin EJ, Loscalzo J, Maron BJ, Maron MS. What causes hypertrophic cardiomyopathy? Am J Cardiol. 2022;179:74–82. doi: 10.1016/j.amjcard.2022.06.017 PubMed DOI PMC
Relationship Between Genotype Status and Clinical Outcome in Hypertrophic Cardiomyopathy
